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I had planned to blast the news of the use of gene-editing to save a British baby from aggressive leukemia. “Two months later, Layla was cancer-free,” proclaimed one of many enthusiastic reports.
I’m always skeptical when I hear the words “cancer” and “cure” in the same sentence, let alone uttered so soon after treatment and without an accompanying technical paper so I can see the data. But when I considered the timing of unfolding events, I realized that the seemingly premature reporting of Layla’s rapidly restored health just might add an important point to the heated discussion over gene and genome editing. That is, can we keep the promising clinical applications on somatic cells, while forbidding the Frankenstein scenarios of germline manipulation?
Related on the SLP
In the rush to get stories out, some media reports muddled gene editing and gene therapy. I noticed right away that the first sentence of the Wall Street Journal article linked “gene-editing technique” to an article about the very gene therapy that I wrote my book about, for a form of hereditary blindness. It adds a gene that doesn’t integrate into a chromosome. Other gene therapies stick the healing genes into chromosomes somewhat randomly. Gene editing, in contrast, switches out or replaces a gene at its precise location in a chromosome. The distinction isn’t just genetic jargon — it could mean the difference between a sustained effect and one that fades as modified cells divide.
Read full, original post: Will Layla Save Gene Editing?
